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  • Title: [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].
    Author: Rethoré MO, Prieur M, de Blois MC, Naffah J, Ravel A, Villain E, Lejeune J.
    Journal: Ann Genet; 1985; 28(3):149-53. PubMed ID: 3879147.
    Abstract:
    The detection of a familial translocation, t(10;18)(p12;q22), has made possible the observation in type and countertype of two related persons with opposite chromosomal imbalance: trisomy 18q22----18qter with monosomy 10p12----10pter in one of the two and monosomy 18q22----10pter in the other. In each case the abnormalities attributable to monosomy overrule those attributable to monosomy overrule those attributable to the associated trisomy.
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